Premium
Identification of regioisomers and enantiomers of triacylglycerols in different yeasts using reversed‐ and chiral‐phase LC – MS
Author(s) -
Řezanka Tomáš,
Kolouchová Irena,
Čejková Alena,
Cajthaml Tomáš,
Sigler Karel
Publication year - 2013
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.201300657
Subject(s) - structural isomer , palmitoleic acid , chemistry , enantiomer , yarrowia , chromatography , propanoic acid , atmospheric pressure chemical ionization , stereochemistry , fatty acid , yeast , organic chemistry , chemical ionization , linoleic acid , biochemistry , ionization , ion
LC with atmospheric pressure chemical ionization (ACPI) MS with RP and chiral phase was used for separation of triacylglycerols ( TAG s) from yeasts of the genera C andida , K luyveromyces , R hodotorula , S accharomyces , T orulospora , T richosporon , and Y arrowia . Chiral LC – APCI ‐ MS is based on using two columns in series packed with a 3,5‐dimethylphenyl carbamate modified β‐cyclodextrin chiral phase. All regioisomers and enantiomers of TAG s containing one to five double bonds were separated. Molecular species of TAG s, i.e. regioisomers and enantiomers, were identified and quantified by MS / MS . Among the 94 identified TAG s, the most abundant were triolein, oleopalmitoleoolein, and dipalmitoleoolein. In strains producing palmitoleic acid in amounts >25% of total fatty acids ( FA s), this acid, or unsaturated FA is bound in sn ‐1. In strains containing palmitoleic acid at 10–25% total FA s this acid is mainly bound in sn ‐3, saturated FA being bound in sn ‐1. Strains containing <10% palmitoleic acid form preferentially symmetrical TAG s.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom